Asay Matthew, Morales-Morales David
Instituto de Quimica, Universidad Nacional Autonoma de Mexico, Circuito Exterior S/N, Cuidad Universitaria Coyoacan, C.P. 04510, Mexico D.F., Mexico.
Dalton Trans. 2015 Oct 28;44(40):17432-47. doi: 10.1039/c5dt02295a. Epub 2015 Sep 23.
Pincer ligands have become ubiquitous in organometallic chemistry and homogeneous catalysis. Recently, new varieties of pincer ligands with non-symmetrical backbones and/or ligating groups have been reported and their application in transition metal complexes has been exploited in a variety of catalytic transformations. This non-symmetric approach vastly increases the structural and electronic diversity of this class of ligand. This approach has proven beneficial in a variety of ways, such as the use of a single weakly coordinating moiety, which can dissociate and thereby create a vacant coordination site to increase the catalyst activity. Additionally, this provides further access to chiral ligands and complexes for asymmetric induction. This perspective highlights recent, important examples of non-symmetric pincer ligands, which feature aryl or pyridine backbones, and the synthesis and use of subsequent complexes in catalytic transformations, and discusses the future potential of this type of ligand system.
钳形配体在有机金属化学和均相催化中已无处不在。最近,已报道了具有非对称骨架和/或配位基团的新型钳形配体,并已在各种催化转化中探索了它们在过渡金属配合物中的应用。这种非对称方法极大地增加了这类配体的结构和电子多样性。这种方法已在多种方面证明是有益的,例如使用单个弱配位部分,其可以解离从而产生一个空的配位位点以提高催化剂活性。此外,这为不对称诱导提供了进一步获得手性配体和配合物的途径。本综述重点介绍了具有芳基或吡啶骨架的非对称钳形配体的近期重要实例,以及后续配合物在催化转化中的合成和应用,并讨论了这类配体体系的未来潜力。